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Consensus Rules in Variant Detection from Next-Generation Sequencing Data
A critical step in detecting variants from next-generation sequencing data is post hoc filtering of putative variants called or predicted by computational tools. Here, we highlight four critical parameters that could enhance the accuracy of called single nucleotide variants and insertions/deletions:...
Gorde:
| Egile Nagusiak: | , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Public Library of Science
2012
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3371040/ https://ncbi.nlm.nih.gov/pubmed/22715385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0038470 |
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